Hove-Madsen L, Méry P F, Jurevicius J, Skeberdis A V, Fischmeister R
INSERM U-446, Université de Paris-Sud, Faculté d Pharmacie, Châtenay-Malabry, France.
Basic Res Cardiol. 1996;91 Suppl 2:1-8. doi: 10.1007/BF00795355.
Hormonal regulation of cardiac inotropism is often correlated with modification of the L-type Ca-channel current. Among several regulatory pathways that control Ca-channel activity, the best described one is the cAMP cascade. Cyclic AMP-dependent phosphorylation of the Ca-channel results in an increase of the mean open probability of the individual Ca-channels and, thus, of the macroscopic Ca current. Modulation of cAMP concentration can take place at the level of adenylyl cyclases or cAMP phosphodiesterases. Of major interest is the fact that the activity of two different forms of phosphodiesterases is controlled by the level of intracellular cGMP. Thus, cAMP metabolism is intimately associated with cGMP metabolism, and both determine the degree of cAMP-dependent phosphorylation of cardiac Ca-channels. This brief discussion will focus on these two levels of control and their relative importance in the cAMP-dependent regulation of myocardial Ca-channels.
心脏收缩力的激素调节通常与L型钙通道电流的改变相关。在控制钙通道活性的几种调节途径中,描述最清楚的是cAMP级联反应。钙通道的环磷酸腺苷(cAMP)依赖性磷酸化导致单个钙通道的平均开放概率增加,进而使宏观钙电流增加。cAMP浓度的调节可发生在腺苷酸环化酶或cAMP磷酸二酯酶水平。一个主要的关注点是,两种不同形式的磷酸二酯酶的活性受细胞内cGMP水平的控制。因此,cAMP代谢与cGMP代谢密切相关,二者共同决定心脏钙通道cAMP依赖性磷酸化的程度。本简要讨论将聚焦于这两个控制水平及其在心肌钙通道cAMP依赖性调节中的相对重要性。